A report of clinicians’ attitude survey of acquired hemophilia A in daily clinical practice
Author:
Affiliation:
1. Department of Hematology, Uonuma Institute of Community Medicine, Niigata University Medical and Dental Hospital
2. Department of Hematology, Endocrinology and Metabolism, Niigata University Faculty of Medicine
Publisher
Japanese Society on Thrombosis and Hemostasis
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjsth/28/4/28_2017_JJTH_28_4_510-517/_pdf
Reference8 articles.
1. 2) Tiede A, Klamroth R, Scharf RE, Trappe RU, Holstein K, Huth-Kühne A, Gottstein S, Geisen U, Schenk J, Scholz U, Schilling K, Neumeister P, Miesbach W, Manner D, Greil R, von Auer C, Krause M, Leimkühler K, Kalus U, Blumtritt JM, Werwitzke S, Budde E, Koch A, Knöbl P: Prognostic factors for remission of and survival in acquired hemophilia A (AHA): results from the GTH-AH 01/2010 study. Blood 125: 1091–1097, 2015.
2. 5) Collins PW, Hirsch S, Baglin TP, Dolan G, Hanley J, Makris M, Keeling DM, Liesner R, Brown SA, Hay CR; UK Haemophilia Centre Doctors’ Organisation: Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors’ Organisation. Blood 109: 1870–1877, 2007.
3. 6) Green D, Lechner K: A survey of 215 non-hemophilic patients with inhibitors to Factor VIII. Thromb Haemost 45: 200–203, 1981.
4. 7) Lawless S, Benson G: A 75-year-old woman with acquired haemophilia disguised by warfarin treatment. BMJ Case Rep 2015 Oct 6; 2015. pii: bcr2015211254. doi: 10.1136/bcr-2015-211254.
5. 8) Patel N, Wyrko Z, Naqvi S, Croft AP: Acquired haemophilia A: the importance of early recognition in cases of spontaneous bleeding in the elderly. BMJ Case Rep 2014 Nov 20; 2014. pii: bcr2014206911. doi: 10.1136/bcr-2014-206911.
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